Ameditech recalls QuickTox 5 Panel Drug Screen DipCard (P/N QT11, Lot 188787) due to potential false results. Affected users should contact for replacement.
Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744)
Ameditech is recalling QuickTox 5 Panel Drug Screen DipCards with specific product numbers because they may give false results. This could lead to incorrect drug screening outcomes.
The recalled DipCards may produce false positive or negative results when used for drug screening. This could lead to incorrect conclusions about drug use.
People who purchased or use the QuickTox 5 Panel Drug Screen DipCard with product number QT11 and lot number 188:8787 are affected. Those using the product for drug testing are most at risk.
Check for product number QT11 and lot number 188787 on the QuickTox 5 Panel Drug Screen DipCard. The product was sold by Ameditech Inc.
Verify the product number (QT11) and lot number (188787) on the DipCard.
The product number is QT11.
Lot number 188787.
The recall record does not specify replacement instructions.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-0692-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-0692-2020 from Ameditech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
